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Structure of 2761968-90-3
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This boronate ester features a tert-butyl carbamate-protected amine paired with a fluoro-substituted benzo[b]thiophene scaffold, enabling stable coupling in Suzuki-Miyaura reactions. The tetramethyl-1,3,2-dioxaborolane moiety ensures high reactivity and shelf-life under standard conditions.
tert-Butyl (3-cyano-7-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophen-2-yl)carbamate serves as a versatile boron-containing building block for Suzuki-Miyaura coupling reactions. The 4,4,5,5-tetramethyl-1,3,2-dioxaborolane moiety enables stable, room-temperature handling and broad functional group tolerance. The cyano and fluoro substituents provide electronic modulation and synthetic handles for downstream derivatization. This compound facilitates efficient construction of complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: